Canonical Allele Identifier: CA378294121

Gene: BAG3

Linked Data

• ClinVar Variation Id: 505229
• ClinVar RCV Id: RCV001008646 ; RCV002413693 ; RCV002483674 ; RCV003389249
• dbSNP Id: rs1554875409
• gnomAD v4: 10-119651752-G-A
• MyVariant Identifiers: chr10:g.121411264G>A (hg19) ; chr10:g.119651752G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119651752G>A , CM000672.2:g.119651752G>A	GRCh38
NC_000010.10:g.121411264G>A , CM000672.1:g.121411264G>A	GRCh37
NC_000010.9:g.121401254G>A	NCBI36
NG_016125.1:g.5383G>A , LRG_742:g.5383G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000369085.8:c.77G>A MANE Select	ENSP00000358081.4:p.Trp26Ter
ENST00000369085.7:c.77G>A	ENSP00000358081.3:p.Trp26Ter
NM_004281.3:c.77G>A , LRG_742t1:c.77G>A	NP_004272.2:p.Trp26Ter
XM_005270287.1:c.77G>A	XP_005270344.1:p.Trp26Ter
XM_005270287.2:c.77G>A	XP_005270344.1:p.Trp26Ter
NM_004281.4:c.77G>A MANE Select	NP_004272.2:p.Trp26Ter